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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:30:48 UTC
Update Date2022-03-07 02:52:11 UTC
HMDB IDHMDB0029505
Secondary Accession Numbers
  • HMDB29505
Metabolite Identification
Common NameKuwanon A
DescriptionKuwanon A belongs to the class of organic compounds known as 3-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3-position. Thus, kuwanon a is considered to be a flavonoid. Based on a literature review a significant number of articles have been published on Kuwanon A.
Structure
Data?1582753428
Synonyms
ValueSource
5,7-Dihydroxy-2-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl)-3-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one, 9ciHMDB
Chemical FormulaC25H24O6
Average Molecular Weight420.4545
Monoisotopic Molecular Weight420.1572885
IUPAC Name5,7-dihydroxy-2-(5-hydroxy-2,2-dimethyl-2H-chromen-8-yl)-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one
Traditional Namekuwanon A
CAS Registry Number62949-77-3
SMILES
CC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C2OC(C)(C)C=CC2=C(O)C=C1
InChI Identifier
InChI=1S/C25H24O6/c1-13(2)5-6-16-22(29)21-19(28)11-14(26)12-20(21)30-23(16)17-7-8-18(27)15-9-10-25(3,4)31-24(15)17/h5,7-12,26-28H,6H2,1-4H3
InChI KeyDBUNRZUFILGKHP-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 3-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavones
Direct Parent3-prenylated flavones
Alternative Parents
Substituents
  • 3-prenylated flavone
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Hydroxyflavonoid
  • 2,2-dimethyl-1-benzopyran
  • Chromone
  • Benzopyran
  • 1-benzopyran
  • 1-hydroxy-2-unsubstituted benzenoid
  • Pyranone
  • 1-hydroxy-4-unsubstituted benzenoid
  • Alkyl aryl ether
  • Benzenoid
  • Pyran
  • Heteroaromatic compound
  • Vinylogous acid
  • Oxacycle
  • Ether
  • Organoheterocyclic compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.012 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0045 g/LALOGPS
logP4.93ALOGPS
logP5.22ChemAxon
logS-5ALOGPS
pKa (Strongest Acidic)6.61ChemAxon
pKa (Strongest Basic)-4.8ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area96.22 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity120.87 m³·mol⁻¹ChemAxon
Polarizability44.92 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+202.09730932474
DeepCCS[M-H]-199.70130932474
DeepCCS[M-2H]-232.58430932474
DeepCCS[M+Na]+208.00930932474
AllCCS[M+H]+200.232859911
AllCCS[M+H-H2O]+197.432859911
AllCCS[M+NH4]+202.832859911
AllCCS[M+Na]+203.532859911
AllCCS[M-H]-199.932859911
AllCCS[M+Na-2H]-199.532859911
AllCCS[M+HCOO]-199.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Kuwanon ACC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C2OC(C)(C)C=CC2=C(O)C=C14973.3Standard polar33892256
Kuwanon ACC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C2OC(C)(C)C=CC2=C(O)C=C13567.8Standard non polar33892256
Kuwanon ACC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C2OC(C)(C)C=CC2=C(O)C=C13649.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Kuwanon A,1TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O3520.8Semi standard non polar33892256
Kuwanon A,1TMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C3=C2OC(C)(C)C=C3)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O3485.8Semi standard non polar33892256
Kuwanon A,1TMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O)=CC(O)=C2C1=O3512.6Semi standard non polar33892256
Kuwanon A,2TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O3432.9Semi standard non polar33892256
Kuwanon A,2TMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O3417.0Semi standard non polar33892256
Kuwanon A,2TMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O3395.3Semi standard non polar33892256
Kuwanon A,3TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O3398.2Semi standard non polar33892256
Kuwanon A,1TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O3765.4Semi standard non polar33892256
Kuwanon A,1TBDMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C3=C2OC(C)(C)C=C3)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O3727.7Semi standard non polar33892256
Kuwanon A,1TBDMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O)=CC(O)=C2C1=O3773.5Semi standard non polar33892256
Kuwanon A,2TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O3905.6Semi standard non polar33892256
Kuwanon A,2TBDMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O3875.6Semi standard non polar33892256
Kuwanon A,2TBDMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O3868.2Semi standard non polar33892256
Kuwanon A,3TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C3=C2OC(C)(C)C=C3)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O4043.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Kuwanon A GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4i-3009700000-74107fe13021d51fe3832017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kuwanon A GC-MS (3 TMS) - 70eV, Positivesplash10-00di-2100049000-d649803fec7288db50ca2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kuwanon A GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Kuwanon A GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 10V, Positive-QTOFsplash10-00di-1013900000-ff753e13227faa2d1db22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 20V, Positive-QTOFsplash10-014i-2019300000-1e7fb75288ea0ee30e2c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 40V, Positive-QTOFsplash10-0gdj-5294000000-ce183efe5857bb17db732016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 10V, Negative-QTOFsplash10-014i-0000900000-e14bcceaa7e58f511a822016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 20V, Negative-QTOFsplash10-014i-0006900000-fab01c3029bc984c81fd2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 40V, Negative-QTOFsplash10-0k9i-1839100000-cccb242575256566e1252016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 10V, Negative-QTOFsplash10-014i-0000900000-e89f00937a4f746a0b2c2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 20V, Negative-QTOFsplash10-014i-0000900000-e89f00937a4f746a0b2c2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 40V, Negative-QTOFsplash10-0a4i-0609200000-67f18785bb351f49916e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 10V, Positive-QTOFsplash10-00di-0000900000-2c722d7f3ff1673a173f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 20V, Positive-QTOFsplash10-00di-0000900000-2c722d7f3ff1673a173f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Kuwanon A 40V, Positive-QTOFsplash10-0uk9-0960600000-58be6e708439ce7389d12021-09-22Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB000640
KNApSAcK IDC00004057
Chemspider ID24843910
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound44258296
PDB IDNot Available
ChEBI ID1242612
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1810031
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .